AlbuRx
- Product NDC
- 44206-251
- Requested package NDC
- 44206-251-05
- 11-digit product format
- 442060251
- Labeler code
- 44206
- Product ID
- 44206-251_4ab3fa50-584a-43fd-a729-472240f3dc3f
- Type
- PLASMA DERIVATIVE
- Nonproprietary name
- ALBUMIN (HUMAN)
- Dosage form
- SOLUTION
- Route
- INTRAVENOUS
- Labeler
- CSL Behring AG
- Application
- BLA102366
- Marketing category
- BLA
- Marketing start
- 2009-01-06
- Substance
- ALBUMIN HUMAN
- Active strength
- 12.5 g/50mL
- Pharmacologic classes
- Human Serum Albumin [EPC], Increased Intravascular Volume [PE], Increased Oncotic Pressure [PE], Osmotic Activity [MoA], Serum Albumin [Chemical/Ingredient]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- AlbuRx
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALBUMIN HUMAN | 12.5 g/50mL |
Harmonized UNII identifiers#
UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table| Identifier | FDA.report destination |
|---|
| ZIF514RVZR | Internal UNII lookup |
Harmonized RxCUI identifiers#
RxCUI identifiers page 1 of 1 · 4 matching rows.
Identifier, FDA.report destination table| Identifier | FDA.report destination |
|---|
| 1741375 | Internal RxNorm lookup |
| 1741380 | Internal RxNorm lookup |
| 1742404 | Internal RxNorm lookup |
| 1742406 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 44206-251-05 | AlbuRx | 1 in 1 CARTON | SOLUTION | 1 | | 11 |
| 44206-251-10 | AlbuRx | 1 in 1 CARTON | SOLUTION | 1 | | 11 |
| 44206-251-90 | AlbuRx | 50 mL in 1 VIAL, GLASS | SOLUTION | 50 | | 11 |
| 44206-251-91 | AlbuRx | 100 mL in 1 VIAL, GLASS | SOLUTION | 100 | | 11 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 44206-251 | ALBURX (ALBUMIN (HUMAN)) SOLUTION [CSL BEHRING AG] | 11 | Current NDC, Legacy NDC, 4 package rows | 20220811_ad74b7f5-b380-47ab-b19d-eef92c8eb7a4.zip |
Purple Book Biologic Products#
BLA, Proprietary name, Proper name table| BLA | Proprietary name | Proper name | License type | Status | Latest source |
|---|
| 102366 | Alburx | Albumin (Human) | 351(a) | Rx | 2026-10-01 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 44206-251-05 | 44206025105 | 1 VIAL, GLASS in 1 CARTON (44206-251-05) / 50 mL in 1 VIAL, GLASS (44206-251-90) | 2009-01-06 | 0000-00-00 | No | No | Current |